The Safety Rates Drug Report

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Drug     Injury     Quarter    

Person who experienced the adverse event (patient)

Event ID CASE I F COD FOLL SEQ IMAGE EVENT DT MFR DT FDA DT REPT COD MFR NUM MFR SNDR AGE AGE COD GNDR COD E SUB WT WT COD REPT DT OCCP COD DEATH DT TO MFR CONFID REPORTER COUNTRY
5198124 6154495 F 5198124-7 20060928 20070102 20070104 EXP IL-ROCHE-468147 ROCHE 53 YR M Y 86 KG 20070104 MD 20061007 UNITED KINGDOM

Drug(s) used by person

Event ID DRUG SEQ ROLE COD DRUGNAME VAL VBM ROUTE DOSE VBM DECHAL RECHAL LOT NUM EXP DT NDA NUM
5198124 1008009007 PS GANCICLOVIR SODIUM 1 INTRAVENOUS FORM: INJECTION 19661
5198124 1008009008 SS CEREPRO 2 OTHER ROUTE: INJECTION FORM: INJECT DOSE FREQUENCY: SINGLE 1X10 12 VP; REGIMEN # 1
5198124 1008009009 C MANNITOL 1 DRUG: MANNITOL 201
5198124 1008009010 C DEXAMETHASONE 1
5198124 1008009011 C EPANUTIN 2
5198124 1008009012 C FAMOTIDINE 1
5198124 1008009013 C ENOXAPARIN SODIUM 1

Indications of drugs used

Event ID DRUG SEQ INDI PT
5198124 1008009007 GLIOMA
5198124 1008009008 GLIOMA

Outcome of event

Event ID OUTC COD
5198124 DE
5198124 HO
5198124 LT

Reactions reported

Event ID PT
5198124 DYSPHASIA
5198124 INFARCTION
5198124 VEIN DISORDER

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

Event ID DRUG SEQ START DT END DT DUR DUR COD
5198124 1008009007 20061002 20061004 3 DAY
5198124 1008009008 20060928 20060928 1 DAY
5198124 1008009009 20060927
5198124 1008009010 20060921
5198124 1008009011 20060922 20061007 16 DAY
5198124 1008009012 20060921 20060928 8 DAY
5198124 1008009013 20060921